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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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1-Fluoro-4-nitronaphthalene → 4-Fluoronaphthalen-1-amine

HRID 266863
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인쇄 미리보기

반응식

HRID 266863 반응식
[F:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5]([N+:12]([O-])=O)=[CH:4][CH:3]=1>CCOC(C)=O.[Pd]>[F:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5]([NH2:12])=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 2617641-Fluoro-4-nitronaphthalene

생성물 1

HCID 152494054-Fluoronaphthalen-1-amine

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 8857Ethyl Acetate용매

실험 절차

4-Fluoro-1-nitro-naphthalene (1 g) was dissolved in EtOAc (20 mL) and placed into a hydrogenating flask containing Palladium on activated charcoal (10%, 0.3 g). The reaction mixture was hydrogenated at 50 psi for 5 hr. During the reaction, the pressure of the hydrogen dropped due to the consuming of the hydrogen, and it was brought back to 50 psi a few times. Finally, the reaction stopped when all the starting material was used. The resulting solution was filtered through a pad of celite and washed with EtOAc (20 mL). The clear filtrate was concentrated and dried under vacuum to yield 4-Fluoro-1-aminonaphthalene.

후처리

  1. customplaced into a hydrogenating flask
  2. customDuring the reaction
  3. customthe pressure of the hydrogen dropped due to the consuming of the hydrogen, and it
  4. filtrationThe resulting solution was filtered through a pad of celite
  5. washwashed with EtOAc (20 mL)
  6. concentrationThe clear filtrate was concentrated
  7. customdried under vacuum

출처 및 근거

ORD 기록
ord-3487040c7d894b0e9df3b1dbab112100
출처 데이터셋
uspto-grants-1997_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05652269

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